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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 03-12-2015 |
Symbol | CWS3 | ||
Location | 11q23.1 | ||
Name | Cowden syndrome 3 | ||
Corresponding gene | SDHD | ||
Main clinical features |
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Genetic determination
Function/system disorder
| Type
| disease
| |
Remark(s) |